{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "San Diego",
      "address_1": "10020 Pacific Mesa Blvd",
      "reason_for_recall": "Reports where the Low Battery alarm and/or the Very Low Battery alarm are not being triggered before the battery is discharged and all infusion channels are stopped.",
      "address_2": "",
      "product_quantity": "613,800 total units (575,221 units in US)",
      "code_info": "all units",
      "center_classification_date": "20170321",
      "distribution_pattern": "Worldwide distribution.  US nationwide, Europe, Australia, New Zealand, South Africa, Greater Asia, Middle East, and Canada.",
      "state": "CA",
      "product_description": "Alaris System PC unit, model no. 8000 and 8015.  The central programming, monitoring and power supply component for the Alaris infusion pump System.",
      "report_date": "20170329",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "CareFusion 303, Inc.",
      "recall_number": "Z-1520-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75353",
      "termination_date": "20200424",
      "more_code_info": "",
      "recall_initiation_date": "20161101",
      "postal_code": "92121-4386",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}